Bellagio Childrens Sunscreen SPF 45 description, usages, side effects, indications, overdosage, supplying and lots more!

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Bellagio Childrens Sunscreen SPF 45

Lifetech Resources, LLC

BELLAGIO CHILDREN'S SUNSCREEN LOTION SPF 45


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

DRUG FACTS

ACTIVE INGREDIENTS

Homosalate 14.00%, Octinoxate 6.50%, Octisalate 5.00%, Oxybenzone 5.00%, Zinc Oxide 2.74%

PURPOSE

Sunscreen

USE

Helps prevent sunburn. Higher SPF gives more sunburn protection.

DIRECTIONS FOR USE

Apply evenly and liberally to all exposed areas before sun exposure. Ensure complete coverage. Reapply as needed or after swimming, towel drying, perspiring, or vigorous activity. Ask a doctor before use on children under 6 months of age.

WARNING

For external use only.

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENTS

Water, Caprylic/Capric Triglyceride, Acrylates Copolymer, Cyclopentasiloxane, Polysorbate 60, Cetearyl Alcohol, Ceteareth-20, Glycerin, Potassium Cetyl Phosphate, Sorbitan Stearate, VP/Hexadecene Copolymer, Polysorbate 20, Dimethicone, Butyrospermum Parkii (Shea Butter), Squalane, Panthenol, Sodium PCA, Tocopheryl Acetate, Persea Gratissima (Avocado) Oil, Macadamia Ternifolia Seed Oil, Aloe Barbadensis Leaf Extract, Calendula Officinalis Flower Extract, Chamomilla Recutita (Matricaria) Flower Extract, Xanthan Gum, Triethoxycaprylylsilane, Disodium EDTA, Imidazolidinyl Urea, Sodium Benzoate, Potassium Sorbate.

PRINCIPAL DISPLAY PANEL - 118 ML Tube Label

BELLAGIO®
CHILDREN'S
SUNSCREEN
LOTION
SPF 45

4 FL OZ / 118 ML

Bellagio Childrens Sunscreen SPF 45

Bellagio Childrens Sunscreen SPF 45

Homosalate, Octinoxate, Octisalate, Oxybenzone, and Zinc Oxide LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65643-336
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
HOMOSALATE Homosalate 141.904 mg
OCTINOXATE OCTINOXATE 65.884 mg
OCTISALATE OCTISALATE 50.68 mg
OXYBENZONE OXYBENZONE 50.68 mg
Zinc Oxide Zinc oxide 27.773 mg

Inactive Ingredients

Ingredient Name Strength
water
CETOSTEARYL ALCOHOL
POLYOXYL 20 CETOSTEARYL ETHER
CYCLOMETHICONE 5
SORBITAN MONOSTEARATE
GLYCERIN
potassium cetyl phosphate
POLYSORBATE 60
POLYSORBATE 20
MEDIUM-CHAIN TRIGLYCERIDES
DIMETHICONE
SHEA BUTTER
SODIUM PYRROLIDONE CARBOXYLATE
PANTHENOL
.ALPHA.-TOCOPHEROL ACETATE, D-
Aloe Vera Leaf
AVOCADO
MACADAMIA OIL
CALENDULA OFFICINALIS FLOWER
CHAMOMILE
XANTHAN GUM
EDETATE DISODIUM
SODIUM BENZOATE
POTASSIUM SORBATE
IMIDUREA
Octyltriethoxysilane

Product Characteristics

Color
WHITE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:65643-336-19 118 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2009-02-01


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